A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8368



Internal ID15535496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:46322377..46367035hg38UCSC Ensembl
Outerchr7:46361975..46406633hg19UCSC Ensembl
Outerchr7:46328500..46373158hg18UCSC Ensembl
Outerchr7:46135215..46179873hg17UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3844659
hg1944659
hg1844659
hg1744659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5725
Supporting Variants
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv8368
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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